@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_head {
  this: np:hasAssertion dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_assertion;
    np:hasProvenance dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_provenance;
    np:hasPublicationInfo dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_assertion a np:Assertion .
  
  dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_provenance a np:Provenance .
  
  dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_assertion {
  miriam-gene:6895 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGN1452d6f0e154f1b2e60a660aeaec0f64 sio:SIO_000628 miriam-gene:6895, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_provenance {
  dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_assertion dcterms:description
      "[These observations are further supported by the fact that frameshift mutations of TARBP2 occur in sporadic and hereditary carcinomas with microsatellite instability and that DICER1 mutations are associated with familial pleuropulmonary blastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:21346411;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP252885.RARlpVxm4gvSeR6aFt-b3tl6tQu0luUrEig2g9sdiI6IM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:21+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}